Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

194 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Serum IGF-1 and IGFBP-3 levels in healthy children between 0 and 6 years of age.
Yüksel B, Özbek MN, Mungan NÖ, Darendeliler F, Budan B, Bideci A, Çetinkaya E, Berberoğlu M, Evliyaoğlu O, Yeşilkaya E, Arslanoğlu İ, Darcan Ş, Bundak R, Ercan O. Yüksel B, et al. Among authors: evliyaoglu o. J Clin Res Pediatr Endocrinol. 2011;3(2):84-8. doi: 10.4274/jcrpe.v3i2.17. Epub 2011 Jun 8. J Clin Res Pediatr Endocrinol. 2011. PMID: 21750637 Free PMC article.
Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study.
Baş F, Uyguner ZO, Darendeliler F, Aycan Z, Çetinkaya E, Berberoğlu M, Şiklar Z, Öcal G, Darcan Ş, Gökşen D, Topaloğlu AK, Yüksel B, Özbek MN, Ercan O, Evliyaoğlu O, Çetinkaya S, Şen Y, Atabek E, Toksoy G, Aydin BK, Bundak R. Baş F, et al. Among authors: evliyaoglu o. Endocrine. 2015 Jun;49(2):479-91. doi: 10.1007/s12020-014-0498-1. Epub 2014 Dec 11. Endocrine. 2015. PMID: 25500790
Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome.
Sari E, Bereket A, Yeşilkaya E, Baş F, Bundak R, Aydın BK, Darcan Ş, Dündar B, Büyükinan M, Kara C, Adal E, Akıncı A, Atabek ME, Demirel F, Çelik N, Özkan B, Özhan B, Orbak Z, Ersoy B, Doğan M, Ataş A, Turan S, Gökşen D, Tarım Ö, Yüksel B, Ercan O, Hatun Ş, Şimşek E, Ökten A, Abacı A, Döneray H, Özbek MN, Keskin M, Önal H, Akyürek N, Bulan K, Tepe D, Emeksiz HC, Demir K, Kızılay D, Topaloğlu AK, Eren E, Özen S, Demirbilek H, Abalı S, Akın L, Eklioğlu BS, Kaba S, Anık A, Baş S, Unuvar T, Sağlam H, Bolu S, Özgen T, Doğan D, Çakır ED, Şen Y, Andıran N, Çizmecioğlu F, Evliyaoğlu O, Karagüzel G, Pirgon Ö, Çatlı G, Can HD, Gürbüz F, Binay Ç, Baş VN, Fidancı K, Gül D, Polat A, Acıkel C, Cinaz P, Darendeliler F. Sari E, et al. Among authors: evliyaoglu o. Am J Med Genet A. 2016 Apr;170A(4):942-8. doi: 10.1002/ajmg.a.37498. Epub 2016 Jan 20. Am J Med Genet A. 2016. PMID: 26788866
Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene.
Özcabı B, Tahmiscioğlu Bucak F, Ceylaner S, Özcan R, Büyükünal C, Ercan O, Tüysüz B, Evliyaoğlu O. Özcabı B, et al. Among authors: evliyaoglu o. J Clin Res Pediatr Endocrinol. 2015 Sep;7(3):242-8. doi: 10.4274/jcrpe.2067. J Clin Res Pediatr Endocrinol. 2015. PMID: 26831561 Free PMC article.
Neonatal Diabetes: Two Cases with Isolated Pancreas Agenesis due to Homozygous PTF1A Enhancer Mutations and One with Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome due to KCNJ11 Mutation.
Evliyaoğlu O, Ercan O, Ataoğlu E, Zübarioğlu Ü, Özcabı B, Dağdeviren A, Erdoğan H, De Franco E, Ellard S. Evliyaoğlu O, et al. J Clin Res Pediatr Endocrinol. 2018 Jun 1;10(2):168-174. doi: 10.4274/jcrpe.5162. Epub 2017 Sep 25. J Clin Res Pediatr Endocrinol. 2018. PMID: 28943513 Free PMC article.
194 results